SRX23792873 GSM8119407_r1 SRP492527 PRJNA1082206 SRS20615921 GSM8119407 GSM8119407 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA hiPSCs were dissociated using Accutase and counted to load 10,000 cells into on channel of a 10X Chromium chip. One channel per sample was used. After emulsion cell lysis and RNA was extracted followed by library preparation. Libraries were sent to Novogene for sequencing. Single cell suspensions were passed through 40μm cell strainer (Corning) and concentration was adjusted to 1000 cells/μL. Suspensions were loaded in single-cell-G Chip (10X Genomics) for target output of 10,000 cells per sample. Single-cell droplet capture was performed on the Chromium Controller (10X Genomics). cDNA library preparation was performed in accordance with the Single-Cell 3' v 3.0 or v3.1 protocol. Libraries were evaluated for fragment size and concentration using Agilent HSD5000 ScreenTape System (Agilent). Illumina HiSeq 4000 SRX23792874 GSM8119408_r1 SRP492527 PRJNA1082206 SRS20615922 GSM8119408 GSM8119408 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA hiPSCs were dissociated using Accutase and counted to load 10,000 cells into on channel of a 10X Chromium chip. One channel per sample was used. After emulsion cell lysis and RNA was extracted followed by library preparation. Libraries were sent to Novogene for sequencing. Single cell suspensions were passed through 40μm cell strainer (Corning) and concentration was adjusted to 1000 cells/μL. Suspensions were loaded in single-cell-G Chip (10X Genomics) for target output of 10,000 cells per sample. Single-cell droplet capture was performed on the Chromium Controller (10X Genomics). cDNA library preparation was performed in accordance with the Single-Cell 3' v 3.0 or v3.1 protocol. Libraries were evaluated for fragment size and concentration using Agilent HSD5000 ScreenTape System (Agilent). Illumina HiSeq 4000 SRX23792875 GSM8119409_r1 SRP492527 PRJNA1082206 SRS20615924 GSM8119409 GSM8119409 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA hiPSCs were dissociated using Accutase and counted to load 10,000 cells into on channel of a 10X Chromium chip. One channel per sample was used. After emulsion cell lysis and RNA was extracted followed by library preparation. Libraries were sent to Novogene for sequencing. Single cell suspensions were passed through 40μm cell strainer (Corning) and concentration was adjusted to 1000 cells/μL. Suspensions were loaded in single-cell-G Chip (10X Genomics) for target output of 10,000 cells per sample. Single-cell droplet capture was performed on the Chromium Controller (10X Genomics). cDNA library preparation was performed in accordance with the Single-Cell 3' v 3.0 or v3.1 protocol. Libraries were evaluated for fragment size and concentration using Agilent HSD5000 ScreenTape System (Agilent). Illumina HiSeq 4000 SRX23792876 GSM8119410_r1 SRP492527 PRJNA1082206 SRS20615923 GSM8119410 GSM8119410 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA hiPSCs were dissociated using Accutase and counted to load 10,000 cells into on channel of a 10X Chromium chip. One channel per sample was used. After emulsion cell lysis and RNA was extracted followed by library preparation. Libraries were sent to Novogene for sequencing. Single cell suspensions were passed through 40μm cell strainer (Corning) and concentration was adjusted to 1000 cells/μL. Suspensions were loaded in single-cell-G Chip (10X Genomics) for target output of 10,000 cells per sample. Single-cell droplet capture was performed on the Chromium Controller (10X Genomics). cDNA library preparation was performed in accordance with the Single-Cell 3' v 3.0 or v3.1 protocol. Libraries were evaluated for fragment size and concentration using Agilent HSD5000 ScreenTape System (Agilent). Illumina HiSeq 4000 SRX23792877 GSM8119411_r1 SRP492527 PRJNA1082206 SRS20615925 GSM8119411 GSM8119411 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA hiPSCs were dissociated using Accutase and counted to load 10,000 cells into on channel of a 10X Chromium chip. One channel per sample was used. After emulsion cell lysis and RNA was extracted followed by library preparation. Libraries were sent to Novogene for sequencing. Single cell suspensions were passed through 40μm cell strainer (Corning) and concentration was adjusted to 1000 cells/μL. Suspensions were loaded in single-cell-G Chip (10X Genomics) for target output of 10,000 cells per sample. Single-cell droplet capture was performed on the Chromium Controller (10X Genomics). cDNA library preparation was performed in accordance with the Single-Cell 3' v 3.0 or v3.1 protocol. Libraries were evaluated for fragment size and concentration using Agilent HSD5000 ScreenTape System (Agilent). Illumina HiSeq 4000 SRX23792878 GSM8119412_r1 SRP492527 PRJNA1082206 SRS20615926 GSM8119412 GSM8119412 RNA-Seq TRANSCRIPTOMIC SINGLE CELL cDNA hiPSCs were dissociated using Accutase and counted to load 10,000 cells into on channel of a 10X Chromium chip. One channel per sample was used. After emulsion cell lysis and RNA was extracted followed by library preparation. Libraries were sent to Novogene for sequencing. Single cell suspensions were passed through 40μm cell strainer (Corning) and concentration was adjusted to 1000 cells/μL. Suspensions were loaded in single-cell-G Chip (10X Genomics) for target output of 10,000 cells per sample. Single-cell droplet capture was performed on the Chromium Controller (10X Genomics). cDNA library preparation was performed in accordance with the Single-Cell 3' v 3.0 or v3.1 protocol. Libraries were evaluated for fragment size and concentration using Agilent HSD5000 ScreenTape System (Agilent). Illumina HiSeq 4000